[1] |
Ding Liu, Yuanyuan Zhu, Shuangxi Gu, Fener Chen.
Application of Flow Chemistry in Halogenation
[J]. Chinese Journal of Organic Chemistry, 2021, 41(3): 1002-1011.
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[2] |
Lai Shilin, Liao Xu, Zhang Hui, Jiang Yan, Liu Yuangang, Wang Shibin, Xiong Xingquan.
Application of 3D Printing Technology in Organic Synthetic Chemistry
[J]. Chin. J. Org. Chem., 2019, 39(7): 1858-1866.
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[3] |
Hou Yadong, Pang Haixia, Yang Chao, HuiYonghai.
Mesoporous MCM-41 Supported Schiff Base-Cu(ClO4)2·6H2O Catalyzed Synthesis of Spiro[indole-thiazolidine] Derivatives
[J]. Chin. J. Org. Chem., 2018, 38(8): 2036-2044.
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[4] |
Hou Yadong, Dong Xiuzhi, Yang Chao, Hui Yonghai, Xie Zhengfeng.
MCM-41 Immobilized H3PW12O40 Catalyzed the Addition-Elimination Reaction of Imine with Malonitrile in Water
[J]. Chin. J. Org. Chem., 2018, 38(7): 1749-1754.
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[5] |
Gao Yunpeng, Wang Jianbo.
Continuous Flow Reaction of Diazo Compounds
[J]. Chin. J. Org. Chem., 2018, 38(6): 1275-1291.
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[6] |
Xing Liuzhuang, Hou Yadong, Xing Xuejian, Hui Yonghai.
MCM-41@Schiff Base-Mn(OAc)2 Catalyzed Synthesis of Xanthene Derivatives in Water
[J]. Chin. J. Org. Chem., 2018, 38(4): 912-918.
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[7] |
Xing Xuejian, Fan Kui, Pang Haixia, Wu Yang, Yang Jinghui, Shi Wei, Xie Zhengfeng, Hui Yonghai.
One-Pot Synthesis of 4-Thiazolidinone Derivatives Catalyzed by Zinc Acetate-Schiff Base Complex Immobilized on Mesoporous Molecular Sieve MCM-41
[J]. Chin. J. Org. Chem., 2016, 36(8): 1942-1947.
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[8] |
Zhou Junjie, Tang Zhike, Zhang Chao, Wang Dongtian, Zhang Kai, Sun Hongbin.
CuCN-TsOH Catalyzed Synthesis of 2-Aryl-4,5-dihydro-1H-imidazoline in a Continuous-Flow Microreactor
[J]. Chin. J. Org. Chem., 2016, 36(11): 2662-2669.
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[9] |
Hui Yonghai, Shi Wei, Xie Shaolei, Wang Changchun, Xie Zhengfeng.
Three-Component Mannich Reaction Catalyzed by MCM-41 Immobilized H3PW12O40 (PW) in Water
[J]. Chin. J. Org. Chem., 2014, 34(6): 1212-1217.
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[10] |
Wang Changchun, Xie Shaolei, Xie Zhengfeng, Hui Yonghai.
Michael Addition Reaction of Malononitrile and α,β-Unsaturated Ketones Catalyzed by Amine Functionalized MCM-41
[J]. Chin. J. Org. Chem., 2013, 33(11): 2391-2395.
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[11] |
Xie Shaolei, Hui Yonghai, Wang Changchun, Xie Zhengfeng.
Research Progress of Schiff Base Modified MCM-41 Catalyst in Organic Reactions
[J]. Chin. J. Org. Chem., 2013, 33(05): 971-981.
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[12] |
Zhao Dongbo.
Updated Applications of Flow Chemistry in Pharmaceutical Synthesis
[J]. Chin. J. Org. Chem., 2013, 33(02): 389-405.
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[13] |
Chen Yongcheng, Xie Shaolei, Xie Zhengfeng.
Friedel-Crafts Reaction of Indoles with Nitroalkenes Catalyzed by Mesoporous Material MCM-41
[J]. Chin. J. Org. Chem., 2012, 32(10): 1970-1974.
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[14] |
Jin Jie, Dong Ling, Zhang Kehua, Liu Jin .
Recent Advances in Microfluidic Synthesis
[J]. Chin. J. Org. Chem., 2012, 32(01): 201-209.
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[15] |
YU La-Meia,XU Qiu-Huab,CAI Ming-Zhong*,a.
Synthesis of MCM-41-Supported Thioether Palladium Complex and Its Catalytic Properties in Carbonylation of Aryl Halides
[J]. Chin. J. Org. Chem., 2008, 28(2): 256-260.
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